SAVANA: reliable analysis of somatic structural variants and copy number aberrations in clinical samples using long-read sequencing
Hillary Elrick(European Bioinformatics Institute), Isidro Cortés‐Ciriano(European Bioinformatics Institute), M. Tanguy(Genomics England), Solange De Noon(Royal National Orthopaedic Hospital), Greg Elgar(Genomics England), Francesc Muyas(European Bioinformatics Institute), Katherine Trevers(Royal National Orthopaedic Hospital), Fernanda Amary(Royal National Orthopaedic Hospital), Carolin M. Sauer(European Bioinformatics Institute), Adam Giess(Jackson Laboratory), Adrienne M. Flanagan(Royal National Orthopaedic Hospital), Katherine Piculell(Boston Children's Hospital), Jose Espejo Valle-Inclán(Champalimaud Foundation), Alona Sosinsky(Genomics England), Roberto Tirabosco(Royal National Orthopaedic Hospital NHS Trust), Timothy M. Freeman(Genomics England), David T. Miller(Boston Children's Hospital), Ângela Afonso(University of Lisbon), Sonia Zumalave(European Bioinformatics Institute), Cláudia C. Faria(University of Lisbon), Rita Cascão(University of Lisbon)
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